Carbon Dioxide-Air Mixture
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Carbon Dioxide-Air Mixture
- Generic name
- CARBON DIOXIDE-AIR MIXTURE
- Manufacturer
- Roberts Oxygen Company, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 71c939d8-9873-4e2b-be53-50d50eeb570f
- SPL ID
- 43cf238d-860f-2acf-e063-6294a90a148e
- Version
- 10
- Effective date
- 2025-11-17
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:12
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 205849 | derived:openfda.application_number |
| application number | NDA205849 | openfda.application_number | |
| brand name | Carbon Dioxide-Air Mixture | openfda.brand_name | |
| generic name | CARBON DIOXIDE-AIR MIXTURE | openfda.generic_name | |
| manufacturer name | Roberts Oxygen Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 46123-016-01 | openfda.package_ndc |
| ndc | product | 46123-016 | openfda.product_ndc |
| ndc11 | package | 46123001601 | derived:openfda.package_ndc |
| rxcui | 999631 | openfda.rxcui | |
| spl id | 43cf238d-860f-2acf-e063-6294a90a148e | id | |
| spl set id | 71c939d8-9873-4e2b-be53-50d50eeb570f | set_id | |
| unii | 142M471B3J | openfda.unii | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.